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Bernt A Engelsen

Showing results (31-40 of 36) with videos related to

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Seizure|July 2, 2016
Status epilepticus secondary to gliomaKristin M Knudsen-Baas, Kjersti N Power, Bernt A Engelsen, et al.
Brain : a Journal of Neurology|April 28, 2006
The spectrum of clinical disease caused by the A467T and W748S POLG mutations: a study of 26 casesCharalampos Tzoulis, Bernt A Engelsen, Wenche Telstad, et al.
Epilepsia|July 20, 2013
Exposure to antiepileptic drugs in utero and child development: a prospective population-based studyGyri Veiby, Anne K Daltveit, Synnve Schjølberg, et al.
Epilepsia|December 20, 2014
Depression and anxiety in women with epilepsy during pregnancy and after delivery: a prospective population-based cohort study on frequency, risk factors, medication, and prognosisMarte Helene Bjørk, Gyri Veiby, Simone C Reiter, et al.
Annals of Neurology|April 6, 2017
Myoclonus epilepsy and ataxia due to KCNC1 mutation: Analysis of 20 cases and K<sup>+</sup> channel propertiesKaren L Oliver, Silvana Franceschetti, Carol J Milligan, et al.
Nature Genetics|November 18, 2014
A recurrent de novo mutation in KCNC1 causes progressive myoclonus epilepsyMikko Muona, Samuel F Berkovic, Leanne M Dibbens, et al.
Pageof 4

Showing results (31-40 of 36) with videos related to

Sort By:
Pageof 4
You have reached the last page of results.This site can display upto 36 results.
Seizure|July 2, 2016
Status epilepticus secondary to gliomaKristin M Knudsen-Baas, Kjersti N Power, Bernt A Engelsen, et al.
Brain : a Journal of Neurology|April 28, 2006
The spectrum of clinical disease caused by the A467T and W748S POLG mutations: a study of 26 casesCharalampos Tzoulis, Bernt A Engelsen, Wenche Telstad, et al.
Epilepsia|July 20, 2013
Exposure to antiepileptic drugs in utero and child development: a prospective population-based studyGyri Veiby, Anne K Daltveit, Synnve Schjølberg, et al.
Epilepsia|December 20, 2014
Depression and anxiety in women with epilepsy during pregnancy and after delivery: a prospective population-based cohort study on frequency, risk factors, medication, and prognosisMarte Helene Bjørk, Gyri Veiby, Simone C Reiter, et al.
Annals of Neurology|April 6, 2017
Myoclonus epilepsy and ataxia due to KCNC1 mutation: Analysis of 20 cases and K<sup>+</sup> channel propertiesKaren L Oliver, Silvana Franceschetti, Carol J Milligan, et al.
Nature Genetics|November 18, 2014
A recurrent de novo mutation in KCNC1 causes progressive myoclonus epilepsyMikko Muona, Samuel F Berkovic, Leanne M Dibbens, et al.
Pageof 4